A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17507517



Internal ID22565465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61600251..61602850hg38UCSC Ensembl
chr8:62512810..62515409hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855624
Supporting Variants
Samples
Known GenesASPH
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17507517
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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